Variant report

Variant	esv19004
Chromosome Location	chr2:10433505-10439183
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:10438135-10438290	HepG2	liver:	n/a	n/a
2	ATF1	chr2:10438054-10438386	K562	blood:	n/a	n/a
3	BHLHE40	chr2:10438094-10438318	K562	blood:	n/a	n/a
4	CBX3	chr2:10434131-10434584	K562	blood:	n/a	n/a
5	CBX3	chr2:10438868-10439245	K562	blood:	n/a	n/a
6	CBX3	chr2:10438884-10439176	K562	blood:	n/a	n/a
7	CBX3	chr2:10437768-10438646	K562	blood:	n/a	n/a
8	CBX3	chr2:10434176-10434548	K562	blood:	n/a	n/a
9	CCNT2	chr2:10438082-10438352	K562	blood:	n/a	chr2:10438132-10438141
10	CEBPB	chr2:10437715-10438418	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr2:10438006-10438446	A549	lung:	n/a	n/a
12	CEBPB	chr2:10438010-10438391	K562	blood:	n/a	n/a
13	CEBPB	chr2:10437611-10438385	HepG2	liver:	n/a	n/a
14	CEBPB	chr2:10437853-10438620	HCT-116	colon:	n/a	n/a
15	CEBPB	chr2:10437928-10438538	A549	lung:	n/a	n/a
16	CEBPB	chr2:10437577-10438429	IMR90	lung:	n/a	n/a
17	CEBPB	chr2:10437665-10438395	A549	lung:	n/a	n/a
18	CEBPB	chr2:10438066-10438258	HepG2	liver:	n/a	n/a
19	CHD2	chr2:10437978-10438419	Hela-S3	cervix:	n/a	n/a
20	CHD2	chr2:10438117-10438286	HepG2	liver:	n/a	n/a
21	CTCF	chr2:10438260-10438410	HAc	cerebellar:	n/a	n/a
22	E2F6	chr2:10438100-10438297	K562	blood:	n/a	n/a
23	EGR1	chr2:10437740-10438560	HCT-116	colon:	n/a	chr2:10438127-10438140 chr2:10438130-10438139 chr2:10438171-10438180 chr2:10438127-10438140
24	EGR1	chr2:10437934-10438316	K562	blood:	n/a	chr2:10438127-10438140 chr2:10438130-10438139 chr2:10438171-10438180 chr2:10438127-10438140
25	EGR1	chr2:10437750-10438611	HCT-116	colon:	n/a	chr2:10438127-10438140 chr2:10438130-10438139 chr2:10438171-10438180 chr2:10438127-10438140
26	EGR1	chr2:10437957-10438294	K562	blood:	n/a	chr2:10438127-10438140 chr2:10438130-10438139 chr2:10438171-10438180 chr2:10438127-10438140
27	ELF1	chr2:10437957-10438511	K562	blood:	n/a	chr2:10438171-10438182
28	ELF1	chr2:10437931-10438589	K562	blood:	n/a	chr2:10438171-10438182
29	ELK1	chr2:10435906-10436106	GM12878	blood:	n/a	n/a
30	ELK1	chr2:10435930-10436126	K562	blood:	n/a	n/a
31	ELK1	chr2:10438021-10438335	Hela-S3	cervix:	n/a	n/a
32	EP300	chr2:10437795-10438625	SK-N-SH	brain:	n/a	n/a
33	EP300	chr2:10437422-10439314	SK-N-SH	brain:	n/a	n/a
34	EP300	chr2:10437971-10438477	HepG2	liver:	n/a	n/a
35	EP300	chr2:10437926-10438396	K562	blood:	n/a	n/a
36	EP300	chr2:10437958-10438602	SK-N-SH_RA	brain:	n/a	n/a
37	EP300	chr2:10437985-10438565	SK-N-SH_RA	brain:	n/a	n/a
38	EP300	chr2:10438071-10438420	Hela-S3	cervix:	n/a	n/a
39	FOS	chr2:10438000-10438405	MCF10A-Er-Src	breast:	n/a	chr2:10438159-10438170 chr2:10438163-10438171 chr2:10438161-10438172
40	FOS	chr2:10437993-10438385	MCF10A-Er-Src	breast:	n/a	chr2:10438159-10438170 chr2:10438163-10438171 chr2:10438161-10438172
41	FOS	chr2:10438000-10438408	MCF10A-Er-Src	breast:	n/a	chr2:10438159-10438170 chr2:10438163-10438171 chr2:10438161-10438172
42	FOS	chr2:10437997-10438406	MCF10A-Er-Src	breast:	n/a	chr2:10438159-10438170 chr2:10438163-10438171 chr2:10438161-10438172
43	FOS	chr2:10437817-10438654	HUVEC	blood vessel:	n/a	chr2:10438159-10438170 chr2:10438163-10438171 chr2:10438161-10438172
44	FOSL1	chr2:10437746-10438646	HCT-116	colon:	n/a	chr2:10438159-10438170 chr2:10438163-10438171 chr2:10438161-10438172
45	FOSL1	chr2:10437975-10438354	K562	blood:	n/a	chr2:10438159-10438170 chr2:10438163-10438171 chr2:10438161-10438172
46	FOSL1	chr2:10437849-10438546	HCT-116	colon:	n/a	chr2:10438159-10438170 chr2:10438163-10438171 chr2:10438161-10438172
47	FOSL1	chr2:10437993-10438345	K562	blood:	n/a	chr2:10438159-10438170 chr2:10438163-10438171 chr2:10438161-10438172
48	FOSL2	chr2:10437910-10438423	HepG2	liver:	n/a	chr2:10438159-10438170 chr2:10438163-10438171 chr2:10438162-10438173
49	FOSL2	chr2:10437872-10438432	SK-N-SH	brain:	n/a	chr2:10438159-10438170 chr2:10438163-10438171 chr2:10438162-10438173
50	FOSL2	chr2:10437946-10438433	HepG2	liver:	n/a	chr2:10438159-10438170 chr2:10438163-10438171 chr2:10438162-10438173

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:10438486-10438536	IMR90	lung:	fetal
2	chr2:10438486-10438536	IMR90	lung:	fetal
3	chr2:10438486-10438536	ovcar-3	ovarian:	n/a
4	chr2:10438486-10438536	GM12892	blood:	n/a
5	chr2:10438486-10438536	HRCEpiC	kidney:	n/a
6	chr2:10438486-10438536	SAEC	small airway:	n/a
7	chr2:10438486-10438536	K562	blood:	n/a
8	chr2:10438486-10438536	HAEpiC	amniotic membrane:	n/a
9	chr2:10438486-10438536	T-47D	breast:	n/a
10	chr2:10438486-10438536	SK-N-SH_RA	brain:	n/a
11	chr2:10438486-10438536	NHDF-neo	bronchial:	n/a
12	chr2:10438486-10438536	HNPCEpiC	eye:	n/a
13	chr2:10438486-10438536	PANC-1	pancreas:	n/a
14	chr2:10438486-10438536	GM12891	blood:	n/a
15	chr2:10438486-10438536	AoSMC	blood vessel:	n/a
16	chr2:10438486-10438536	U87	brain:	n/a
17	chr2:10438486-10438536	RPTEC	kidney:	n/a
18	chr2:10438486-10438536	SK-N-SH	brain:	n/a
19	chr2:10438486-10438536	Caco-2	colon:	n/a
20	chr2:10438486-10438536	AG04450	lung:	fetal
21	chr2:10438486-10438536	GM06990	blood:	n/a
22	chr2:10438486-10438536	MCF10A-Er-Src	breast:	n/a
23	chr2:10438486-10438536	H1-hESC	embryonic stem cell:	embryo
24	chr2:10438486-10438536	HIPEpiC	eye:	n/a
25	chr2:10438486-10438536	HRPEpiC	eye:	n/a
26	chr2:10438486-10438536	MCF-7	breast:	n/a
27	chr2:10438486-10438536	ECC-1	luminal epithelium:	n/a
28	chr2:10438486-10438536	SK-N-MC	brain:	n/a
29	chr2:10438486-10438536	NH-A	brain:	n/a
30	chr2:10438486-10438536	HCPEpiC	choroid plexus:	n/a
31	chr2:10438486-10438536	SKMC	muscle:	n/a
32	chr2:10438486-10438536	HCF	heart:	n/a
33	chr2:10438486-10438536	BE2_C	brain:	n/a
34	chr2:10438486-10438536	A549	lung:	n/a
35	chr2:10438486-10438536	HMEC	breast:	n/a
36	chr2:10438486-10438536	HEK293	kidney:	embryo
37	chr2:10438486-10438536	HepG2	liver:	n/a
38	chr2:10438486-10438536	PrEC	prostate:	n/a
39	chr2:10438486-10438536	HCT-116	colon:	n/a
40	chr2:10438486-10438536	NHBE	bronchial:	n/a
41	chr2:10438486-10438536	HUVEC	blood vessel:	n/a
42	chr2:10438486-10438536	CMK	blood:	n/a
43	chr2:10438486-10438536	Hepatocyte	liver:	n/a
44	chr2:10438486-10438536	ProgFib	skin:	n/a
45	chr2:10438486-10438536	Jurkat	blood:	n/a
46	chr2:10438486-10438536	HCM	heart:	n/a
47	chr2:10438486-10438536	AG09309	skin:	n/a
48	chr2:10438486-10438536	GM19239	blood:	n/a
49	chr2:10438486-10438536	AG09319	gingival:	n/a
50	chr2:10438486-10438536	HRE	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:10436760..10438833-chr2:10575893..10578796,2	K562	blood:
2	chr2:10432073..10436168-chr2:10439823..10445220,6	K562	blood:
3	chr2:10438477..10441704-chr2:10442402..10444544,4	MCF-7	breast:
4	chr2:10436642..10438745-chr2:10547775..10550649,2	K562	blood:
5	chr2:10437138..10439470-chr2:10586145..10589513,3	K562	blood:
6	chr2:10423331..10426574-chr2:10438305..10440403,3	K562	blood:
7	chr2:10405314..10407272-chr2:10438185..10440055,2	K562	blood:
8	chr2:10425416..10427502-chr2:10437383..10439645,2	K562	blood:
9	chr2:10409808..10412548-chr2:10436886..10439745,2	K562	blood:
10	chr2:10434745..10440361-chr2:10440769..10446494,13	MCF-7	breast:

Variant related genes	Relation type
HPCAL1	TF binding region
ENSG00000206898	TF binding region
HPCAL1	CpG island
ENSG00000206898	CpG island
ENSG00000257135	chromatin interactions
ENSG00000206633	chromatin interactions
ENSG00000115758	chromatin interactions
ENSG00000115756	chromatin interactions

Extended variants
information (count: 213 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:213 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs371175844	chr2:10433562-10433563	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs191961035	chr2:10433575-10433576	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs568113881	chr2:10433706-10433707	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs535660109	chr2:10433708-10433709	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs529093928	chr2:10433726-10433727	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs368805242	chr2:10433730-10433731	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs553615643	chr2:10433744-10433745	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs144472322	chr2:10433753-10433754	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs565623188	chr2:10433777-10433778	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs539376727	chr2:10433808-10433809	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs529167251	chr2:10433880-10433881	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs2357540	chr2:10433887-10433888	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs576394288	chr2:10433945-10433946	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs2357541	chr2:10433946-10433947	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs373182384	chr2:10433965-10433966	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs565317424	chr2:10434006-10434007	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs534424739	chr2:10434036-10434037	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs148099317	chr2:10434049-10434050	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs574120124	chr2:10434050-10434051	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs541624789	chr2:10434053-10434054	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs77140785	chr2:10434113-10434114	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs533660504	chr2:10434123-10434124	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs111896789	chr2:10434144-10434145	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs563883459	chr2:10434146-10434147	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs550604298	chr2:10434151-10434152	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs551018925	chr2:10434224-10434225	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs531338697	chr2:10434264-10434265	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs1989563	chr2:10434273-10434274	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs116676008	chr2:10434358-10434359	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs182163251	chr2:10434394-10434395	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs76725818	chr2:10434419-10434420	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs185870803	chr2:10434433-10434434	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs557261870	chr2:10434498-10434499	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs60242178	chr2:10434656-10434657	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs141880440	chr2:10434695-10434696	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs7571627	chr2:10434714-10434715	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs60900876	chr2:10434715-10434716	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs534824959	chr2:10434725-10434726	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs569924691	chr2:10434740-10434741	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs10167820	chr2:10434769-10434770	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs374064897	chr2:10434839-10434840	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs555509324	chr2:10434898-10434899	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs369152543	chr2:10434915-10434916	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs190382326	chr2:10434931-10434932	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs565533895	chr2:10434932-10434933	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs150649749	chr2:10434933-10434934	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs35068336	chr2:10434938-10434939	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs578225250	chr2:10434956-10434957	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs545672700	chr2:10435032-10435033	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs573240670	chr2:10435261-10435262	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Mental retardation	17847001	CNVD
Glioblastoma multiforme	21080181	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Cancer	20164920	CNVD
Neuroblastoma	21508638	CNVD
Breast cancer	17603634	CNVD
Cancer	16751803	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Ependymoma	16718352	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Glioma	17123091	CNVD
Breast cancer	20409316	CNVD
Multiple myeloma	16616336	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Breast cancer	22522925	CNVD
Neuroblastoma	18923524	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:212 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:10426200-10438000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr2:10426800-10437600	Weak transcription	Spleen	Spleen
3	chr2:10429600-10436800	Weak transcription	Monocytes-CD14+_RO01746	blood
4	chr2:10430200-10435400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr2:10430800-10435200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr2:10431000-10433800	Weak transcription	HMEC	breast
7	chr2:10433800-10434000	Enhancers	HMEC	breast
8	chr2:10434000-10437400	Weak transcription	HMEC	breast
9	chr2:10435200-10435800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr2:10435200-10438200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr2:10435200-10438800	Enhancers	Placenta	Placenta
12	chr2:10435400-10435600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr2:10435400-10435800	Enhancers	Stomach Mucosa	stomach
14	chr2:10435400-10438600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr2:10435600-10435800	Enhancers	Sigmoid Colon	Sigmoid Colon
16	chr2:10435600-10437800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr2:10435800-10437600	Weak transcription	Sigmoid Colon	Sigmoid Colon
18	chr2:10435800-10437800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr2:10435800-10441000	Weak transcription	Stomach Mucosa	stomach
20	chr2:10436000-10442000	Enhancers	Primary monocytes fromperipheralblood	blood
21	chr2:10436200-10436600	Enhancers	Placenta Amnion	Placenta Amnion
22	chr2:10436200-10436600	Enhancers	NHEK	skin
23	chr2:10436400-10436600	Enhancers	K562	blood
24	chr2:10436400-10437200	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr2:10436600-10436800	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr2:10436600-10437000	Enhancers	H1 Cell Line	embryonic stem cell
27	chr2:10436600-10437200	Weak transcription	K562	blood
28	chr2:10436600-10437600	Weak transcription	NHEK	skin
29	chr2:10436600-10437800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr2:10436600-10438600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr2:10436600-10442200	Weak transcription	Placenta Amnion	Placenta Amnion
32	chr2:10436800-10437800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
33	chr2:10436800-10437800	Enhancers	Monocytes-CD14+_RO01746	blood
34	chr2:10437000-10437400	Weak transcription	H1 Cell Line	embryonic stem cell
35	chr2:10437000-10438800	Enhancers	Fetal Thymus	thymus
36	chr2:10437000-10439000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr2:10437200-10438200	Weak transcription	HUES48 Cell Line	embryonic stem cell
38	chr2:10437200-10438800	Enhancers	K562	blood
39	chr2:10437400-10437600	Enhancers	H1 Cell Line	embryonic stem cell
40	chr2:10437400-10437600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr2:10437400-10437800	Enhancers	A549	lung
42	chr2:10437400-10438000	Enhancers	Primary hematopoietic stem cells	blood
43	chr2:10437400-10438200	Enhancers	Primary neutrophils fromperipheralblood	blood
44	chr2:10437400-10438200	Enhancers	Primary hematopoietic stem cells short term culture	blood
45	chr2:10437400-10438200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
46	chr2:10437400-10438200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr2:10437400-10438200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr2:10437400-10438600	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr2:10437400-10438600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr2:10437400-10438600	Enhancers	Fetal Muscle Trunk	muscle

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